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A case of Down syndrome with acute lymphoblastic leukemia and isochromosome Xp.

作者信息

Baker Jillian M, Coppes Max J, Roland Birgitte

机构信息

Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.

出版信息

Cancer Genet Cytogenet. 2003 Nov;147(1):75-7. doi: 10.1016/s0165-4608(03)00197-3.

Abstract

A 3-year, 9-month-old girl with trisomy 21 was diagnosed with acute lymphoblastic leukemia (ALL). The karyotype of her leukemic cells at diagnosis-48,XX,+i(X)(p10),+21c-included an extra, structurally abnormal X chromosome as the sole acquired abnormality. While an extra X chromosome is a common abnormality in childhood ALL, it is seldom the only acquired aberration. Furthermore, an additional X chromosome that is structurally abnormal is rare, and has not been reported previously as a solitary abnormality. Here we report a novel karyotype in childhood ALL and review the eight previously described cases of ALL with an extra X isochromosome as the only acquired abnormality.

摘要

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